Package 72888-457-01

Brand: chlorpromazine hydrochloride

Generic: chlorpromazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72888-457-01
Digits Only 7288845701
Product NDC 72888-457
Description

120 mL in 1 BOTTLE (72888-457-01)

Marketing

Marketing Status
Marketed Since 2025-10-10
Brand chlorpromazine hydrochloride
Generic chlorpromazine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4144a379-1c55-ade1-e063-6394a90a66ff", "openfda": {"upc": ["0372888457017", "0372888458014"], "unii": ["9WP59609J6"], "rxcui": ["991053", "991332"], "spl_set_id": ["02c56c39-99bd-44a4-8d9d-9d867c323968"], "manufacturer_name": ["Advagen Pharma Ltd"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 mL in 1 BOTTLE (72888-457-01)", "package_ndc": "72888-457-01", "marketing_start_date": "20251010"}], "brand_name": "chlorpromazine hydrochloride", "product_id": "72888-457_4144a379-1c55-ade1-e063-6394a90a66ff", "dosage_form": "CONCENTRATE", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "72888-457", "generic_name": "chlorpromazine hydrochloride", "labeler_name": "Advagen Pharma Ltd", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "chlorpromazine hydrochloride", "active_ingredients": [{"name": "CHLORPROMAZINE HYDROCHLORIDE", "strength": "30 mg/mL"}], "application_number": "ANDA216678", "marketing_category": "ANDA", "marketing_start_date": "20251010", "listing_expiration_date": "20261231"}